CA2058452A1 - Process for controlling the proportion of air in a hot exhaust-gas stream, and oxygen probe for use in the process - Google Patents
Process for controlling the proportion of air in a hot exhaust-gas stream, and oxygen probe for use in the processInfo
- Publication number
- CA2058452A1 CA2058452A1 CA002058452A CA2058452A CA2058452A1 CA 2058452 A1 CA2058452 A1 CA 2058452A1 CA 002058452 A CA002058452 A CA 002058452A CA 2058452 A CA2058452 A CA 2058452A CA 2058452 A1 CA2058452 A1 CA 2058452A1
- Authority
- CA
- Canada
- Prior art keywords
- oxygen
- probe
- gas stream
- exhaust gas
- oxygen probe
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 239000000523 sample Substances 0.000 title claims abstract description 77
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 title claims abstract description 66
- 239000001301 oxygen Substances 0.000 title claims abstract description 66
- 229910052760 oxygen Inorganic materials 0.000 title claims abstract description 66
- 239000007789 gas Substances 0.000 title claims abstract description 48
- 238000000034 method Methods 0.000 title claims abstract description 16
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 claims abstract description 21
- 239000000203 mixture Substances 0.000 claims abstract description 19
- 238000009792 diffusion process Methods 0.000 claims abstract description 13
- 239000000919 ceramic Substances 0.000 claims abstract description 12
- 238000002485 combustion reaction Methods 0.000 claims abstract description 9
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 8
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 8
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims abstract description 7
- 229910002091 carbon monoxide Inorganic materials 0.000 claims abstract description 7
- 230000001419 dependent effect Effects 0.000 claims abstract description 7
- 238000002360 preparation method Methods 0.000 claims abstract description 5
- 230000001681 protective effect Effects 0.000 claims abstract description 5
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000000446 fuel Substances 0.000 claims description 9
- 229910052751 metal Inorganic materials 0.000 claims description 8
- 239000002184 metal Substances 0.000 claims description 8
- 238000010438 heat treatment Methods 0.000 claims description 4
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 2
- 229910002113 barium titanate Inorganic materials 0.000 claims description 2
- JRPBQTZRNDNNOP-UHFFFAOYSA-N barium titanate Chemical compound [Ba+2].[Ba+2].[O-][Ti]([O-])([O-])[O-] JRPBQTZRNDNNOP-UHFFFAOYSA-N 0.000 claims description 2
- 229910052791 calcium Inorganic materials 0.000 claims description 2
- 239000011575 calcium Substances 0.000 claims description 2
- 239000012535 impurity Substances 0.000 claims description 2
- 229910052712 strontium Inorganic materials 0.000 claims description 2
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 claims description 2
- 239000003792 electrolyte Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- 238000010276 construction Methods 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000007599 discharging Methods 0.000 description 2
- 239000010408 film Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 238000007650 screen-printing Methods 0.000 description 2
- 229910000881 Cu alloy Inorganic materials 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- MCMNRKCIXSYSNV-UHFFFAOYSA-N ZrO2 Inorganic materials O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 229910010293 ceramic material Inorganic materials 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- SIWVEOZUMHYXCS-UHFFFAOYSA-N oxo(oxoyttriooxy)yttrium Chemical compound O=[Y]O[Y]=O SIWVEOZUMHYXCS-UHFFFAOYSA-N 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000010970 precious metal Substances 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- VEALVRVVWBQVSL-UHFFFAOYSA-N strontium titanate Chemical compound [Sr+2].[O-][Ti]([O-])=O VEALVRVVWBQVSL-UHFFFAOYSA-N 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910001868 water Inorganic materials 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
- G01N27/26—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
- G01N27/416—Systems
- G01N27/417—Systems using cells, i.e. more than one cell and probes with solid electrolytes
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
- G01N27/26—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
- G01N27/403—Cells and electrode assemblies
- G01N27/406—Cells and probes with solid electrolytes
- G01N27/407—Cells and probes with solid electrolytes for investigating or analysing gases
- G01N27/4077—Means for protecting the electrolyte or the electrodes
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F02—COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
- F02D—CONTROLLING COMBUSTION ENGINES
- F02D41/00—Electrical control of supply of combustible mixture or its constituents
- F02D41/02—Circuit arrangements for generating control signals
- F02D41/14—Introducing closed-loop corrections
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F02—COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
- F02D—CONTROLLING COMBUSTION ENGINES
- F02D41/00—Electrical control of supply of combustible mixture or its constituents
- F02D41/02—Circuit arrangements for generating control signals
- F02D41/14—Introducing closed-loop corrections
- F02D41/1438—Introducing closed-loop corrections using means for determining characteristics of the combustion gases; Sensors therefor
- F02D41/1439—Introducing closed-loop corrections using means for determining characteristics of the combustion gases; Sensors therefor characterised by the position of the sensor
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F02—COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
- F02B—INTERNAL-COMBUSTION PISTON ENGINES; COMBUSTION ENGINES IN GENERAL
- F02B1/00—Engines characterised by fuel-air mixture compression
- F02B1/02—Engines characterised by fuel-air mixture compression with positive ignition
- F02B1/04—Engines characterised by fuel-air mixture compression with positive ignition with fuel-air mixture admission into cylinder
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F02—COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
- F02B—INTERNAL-COMBUSTION PISTON ENGINES; COMBUSTION ENGINES IN GENERAL
- F02B75/00—Other engines
- F02B75/02—Engines characterised by their cycles, e.g. six-stroke
- F02B2075/022—Engines characterised by their cycles, e.g. six-stroke having less than six strokes per cycle
- F02B2075/027—Engines characterised by their cycles, e.g. six-stroke having less than six strokes per cycle four
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- Immunology (AREA)
- Mechanical Engineering (AREA)
- Molecular Biology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Physics & Mathematics (AREA)
- Analytical Chemistry (AREA)
- Combustion & Propulsion (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- General Engineering & Computer Science (AREA)
- Pathology (AREA)
- Measuring Oxygen Concentration In Cells (AREA)
- Sampling And Sample Adjustment (AREA)
- Exhaust Gas After Treatment (AREA)
- Exhaust Silencers (AREA)
- Combined Controls Of Internal Combustion Engines (AREA)
- Ignition Installations For Internal Combustion Engines (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
- Exhaust Gas Treatment By Means Of Catalyst (AREA)
Abstract
Abstract The method for controlling the fuel-air mixture in an Otto engine having at least one cylinder, especially in an automobile engine, serves for the optimum use of a catalyser (18) with a probe in the hot exhaust gas stream (20) with carbon monoxide, nitrogen oxides and hydrocarbons. The measuring signals of the probe are converted through electronic means into control signals for the mixture preparation and ignition.
The oxygen content of the exhaust gas stream (20) is measured in the combustion chamber of the cylinders, after the outlet valve in the cylinder heads or in the single pipes (12), in the protective region of a smooth, aerodynamic deflection device (40) it is measured without a reference atmosphere with a resistive ceramic oxygen probe (24) having a heat resistance up to approximately 1300°C and an adjustment time within the millisecond range.
The oxygen probe (24) has a specific electrical conductivity dependent upon the oxygen partial pressure.
The sensor layer (32), in the form of a thin diffusion layer, consists of a semi conducting titanate arranged on a small ceramic support (30).
Fig. 3.
The oxygen content of the exhaust gas stream (20) is measured in the combustion chamber of the cylinders, after the outlet valve in the cylinder heads or in the single pipes (12), in the protective region of a smooth, aerodynamic deflection device (40) it is measured without a reference atmosphere with a resistive ceramic oxygen probe (24) having a heat resistance up to approximately 1300°C and an adjustment time within the millisecond range.
The oxygen probe (24) has a specific electrical conductivity dependent upon the oxygen partial pressure.
The sensor layer (32), in the form of a thin diffusion layer, consists of a semi conducting titanate arranged on a small ceramic support (30).
Fig. 3.
Description
2 ~
Control of the air ratio in a hot exhaust gas stream and oxygen probe therefore __________ _____________________________________________ The invention relates to a method for controlling the air-fuel mixture in an Otto engine having at least one cylinder, especially in an automobile engine, for the optimum use of a catalyser with a probe which serves to determine the air ratio in a hot exhaust gas stream with carbon monoxide, nitrogen oxides and hydrocarbons, in which the measuring signals of the probe are converted with an electronic means into control signals for the ignition and mixture preparation. The invention further relates to a d~vice for carrying out the method~
An Otto engine, an engine with a spark ignition, e.g. an automobile petrol engine, a stationary petrol engine or a two-stroke petrol engine, produces essentially carbon dioxide, but also carbon monoxide, nitrogen oxide and hydrocarbons, which are discharged into the environment.
Whereas the carbon monoxide and the nitrogen oxides relate to chemically defined compounds, the hydrocarbons comprise ; a large number of compo~nds.
Automobile engines especially these days are subjected to increasingly strict exhaust gas standards which permit only limited residual quantities of the harmful gases mentioned.
In khe exhaust gas cleaning technology for Otto engines driven by petrol, a central role is played by catalysers controlled by a lambda probe, especially three-way catalysers, but also oxidation andtor twin-bed catalysers.
In a series of chemical reactions, ~or example in a three-way catalyser, the harm~ul exhaust gas components, especially also the heterogenic hydrocarbons, are converted ;~ , , . , ~ . :
' ~, . p '.' . ' ' ' " . ~ 1'.". . , , :
2~8~2 are converted with approxima-tely 90% of efficiency into water, carbon dioxide, nitrogen and hydrogen.
The simultaneous reaction of the harmful exhaust gases of carbon monoxide, nitrogen oxides and hydrocarbons assumes that a ratio of the air-fuel mixture around the stoichiometric value ~ = 1 is adhered to within strict limits. Lambda is also used to represent the air ratio:
air quantity supplied = theoretical air requirement ~ < 1 refers to a rich mixture, ~ ~ 1 refers to a lean mixture.
A lambda probe supplies a voltage signal to an electronic control which in turn signals to a mixture preparation device whether the mixture is to be enriched or made leaner. However, the change in the air-fuel mixture must not take place suddenly, an integrator changes the mixture composition and, if necessary, it changes the ignition timing slowly as a function of time. The air-fuel mixture thus deviates constantly by a few percent around ~ = 1, even during optimum operation.
According to the present-day state of the art, lambda probes are arranged before the catalyser in the exhaust gas flow direction approximately lm down-stream behind the exhaust gas quarter bend, in the collecting pipe in the case of multi-cylinder engines~
A lambda probe operates according to the principle of a galvanic oxygen concentration cell with a solid body electrolyte of zirconium dioxide which is stabilised with yttrium oxide. The solid body electrolyte is protected with a metal mesh - also known as metal cage -, which dampens the force of the hot exhaust gas stream. The exhaust gas 2 ~
flows round the outer surface of the solid body electrolyte, while the inner open chamber is connected to the atmosphere as reference gas.
Despite its obvious advantages , the lambda probe also has disadvantages:
~ It operates only at temperatures from approximately 400C upwards. During the critical period prior to th0 catalyser being heated, the air-fuel mixture is not regulated, or the lambda probe must be pre-heated.
- The maximum continuous operating temperature is approximately 80~C. The probe must be arranged in a cooler area of the collecting pipe, relatively far back in the flow direction.
- The lamda probe has a response time of 50 to 100 msec.
which, together with the long delay of the exhaust gas prior to reaching the probe, amounts to a very long reaction time for engines operating at high speeds.
- The lambda probe provide~ with a metal mesh or metal cage has a large effective cross-section and therefore substantially inter~eres with the exhaust gas stream.
The CH-A5 666 724 describes a lambda probe which has a solid body electrolyte withdrawn from the exhaust gas stream. Whilst the lambda probe seated on a tubular holder is less likely to be overheated and does not interfere with the exhaust gas stream, being situated further back, however, it is even more sluggish with regard to the reaction time, the exhaust gas stream flowing unhindered no longer flows directly round the solid body electrolyte, but only after a branched-off partial stream has passed through a relatively small opening.
'~
;
5C~
The DE-Cl 3 743 295 sets out to prevent the probe ceramics from being destroyed by liquid droplets falling onto a heated lambda probe during cold starting. ~lso, the representation of the si~nals delivered by the lambda probe is intended to be improved. For this purpose a gas deflection plate is arranged upstream of the lambda probe in such a way that the lambda probe is situated in the flow shadow. The lambda probe protected by a relatively large cage of known construction is arranged in the collecting pipe of the exhaust system and captures part of the entire exhaust gas stream of all the cylinders in a region with an already relatively low gas temperature.
It is the object of the present invention to provide a method of the type mentioned at the beginning and a device for carrying the method which permit a more selective engine control with probes and associated control electronics which respond substantially more quickly than was hitherto the case.
With reference to the method, the object according to the invention is achieved in that the oxygen content of the exhaust gas stream is measured in the combustion chamber of the cylinders, after the outlet valve in the cylinder heads, or in the single pipes, by measuring without a re~erence atmosphere in the protective area of a smooth, aerodynamic deflection device with a resistive ceramic oxygen probe having a heat resistance of up to approximately 1300C and an adjustment time within the millisecond ~ange. Special and further developing embodiments are the subject of the dependent patent claims.
The deflection device arranged in the selective cylinder exhaust gas stream simultaneously carries out several functions:
, ~ , .
-- It forms a heat shield for the oxygen probe, which protects against the direct effect of the discharging exhaust gases of very high temperature produced in an explosion-like manner. However, the deflection device which is at least partly open in relation to the exhaust gases downstream in the flow direction ensures that directly and unmixed a part of the exhaust gas stream always flows around the probe. With the oxygen probe arranged in a completely closed or substantially closed deflection device, the advantage of a quick response time would be at least partly cancelled out, similar to an arrangement of a probe according to CH-AS 666724.
- The metal deflection device removes heat from the protective region for the oxygen probe situated in the exhaust gas stream and conducts this to the outside. This improves the heat protection still further.
- Because of the mall dimensions of the probe, the exhaust gas stream is only insignificantly affected even in single pipes by the small construction of the smooth, aerodynamic deflection device and therefore does not af~ect engine efficiency or only insignificantly.
A conventional lambda probe with the necessary protective cage for purely geometric reasons alone could not be arranged in an single pipe and despite deflection plate would never be able to withstand the high temperatures of the method according to the invention.
According to the invention, the oxygen content is measured with an adjustment time of 1 to 20 msec, preferably 3 to 15 msec. With a response time of a few milliseconds, the resistive oxygen probe can measure and adjust the air-fuel mixture of each individual piston stroke even in engines running at high speeds, for example 6000 revolutions per minute. For dynamic drive situations, especially when :~
- . , : ~.
- :~
2 ~
accelerating, with a downstream catalyser the fuel consumption and thus the emission of harmful exhaust gases can be reduced to a minimum. In the first place this is of great significance during the cold starting phase, during which a short response time is essential.
The high degree of heat resistance of the oxygen sensor operating without a reference atmosphere, in cooperation with the smooth, aerodynamic deflection device, allo~s the oxygen content to be measured in the combustion chamber of the cylinders, after the outlet valve in the cylinder heads or in the single pipes of the exhaust system. Of particular practical interest is the measurement of the oxygen ratio directly after the inlet opening of an single pipe of the exhaust system. Only these measuring points, situated outside the operating area of the conventional lambda probes, allow a selected cylinder to be controlled, i.e.
the optîmum combustion in each cylinder.
For the sake of completeness, it is emphasised once more that with the classical lambda probes the oxygen content of the exhaust gas stream can only be measured in the collecting pipe of the exhaust system Because of the deflection device, the oxygen probe as a rule has an adequate heat resistance up to approximately 1300C even in very hot parts of the engine. In the said preferred re~ion for measuring the oxygen content, the inlet region to the single pipes, the temperature as a rule is around 900 to 1100C.
Although resistive ceramic oxygen probes start to react at a temperature of 20C, an arrangement in hot to very hot exhaust gases i6 advantageous, because the delay time is shortest after ignition of the gases until the exhaust i gases reach the oxygen probe and, for adjusting the oxygen : . ~ ,, ~
,, , :. - , , :
2~5~
content, the optimum permanent temperature of the oxygen probe for regulating the air-fuel mixture is quickly reached.
The further simplification of the measuring method is helped by the fact that a resistive oxygen probe operating without a reference atmosphere, apart from high temperatures, is also resistant to high pressures without affecting the quick response time within the millisecond range.
With reference to the device, the object is achieved according to the invention in that an oxygen probe with specific electrical conductivity dependent on the oxygen partial pressure, as the thin diffusion layer of a semi-conducting titanate on a small ceramic support, is arranged on the leeward side of an aerodynamic deflection surface which is at least partly open downstream in the combustion chamber of the cylinder, after the outlet valve in the cylinder heads or in the single pipes. Special and further developing embodiments are the subject of the dependent patent claims.
The active layer of the oxygen sensor preferably has a two-dimensional expansion of from 0,5 to 10 mm2 and a thickness of 1 to 20 ~m, especially 5 to 10 ~m. The application preferably takes place by thin or thick-film technology.
An oxygen sensor of small dimensions, which is known per se and which is freely available, is of considerable significance for a number of reasons:
:' .
- The sensor adjustment time i6 dependent on the layer thickness; the thinner the layer, the shorter the adjustment time.
i ~ - The flow behaviour of the exhaust gases should be .. ~
.--- ..
.
2 ~
disturbed as little as possible by the oxygen probe. This can best be achieved by a deflection surface in which the sensor to be protected is as small as possible. The closer the oxygen probe is arranged to a combustion chamber, the more important become flow optimisation and thus, according to the invention, an 0ffective combination of deflection surface and oxygen probe for producing a homogenous flow around the same.
- Smaller oxygen probes and thus smaller deflection surfaces result in smaller manufacturing and assembly costs.
The diffusion layer which absorbs oxygen in proportion to the partial pressure preferably consists of calcium, strontium or barium titanate with doping material known per se. The conductivity as a function of the oxygen partial pressure is the result of a change in the concentration of atomic defects. Because of its direct dependence on the oxygen partial pressure, this electric conductivity requires no reference atmosphere.
Newly fitted or exchanged oxygen probes preferably have an oxygen-absorbing diffusion layer which already contains the impurities present in the exhaust gas stream. A balance therefore always exists right from the start, which therefore immediately allows an optimum adjustment of the oxygen content even during a refit.
The oxygen probe and the deflection surface are preferably constructed as one module to be rigidly fitted or which can preferably be exchanged.
The deflection surface is made from a heat-resistant and corrosion-proof material which is also abrasion-resistant, preferably from a metal and/or ceramic material which is smooth and aerodynamically shaped in order to reduce the 2 ~ r~ 2 flow resistance. A deflection plate, e.g. forming the deflection surface, made from metal, preferably a heat-conducting steel or a copper alloy is preferably connected in a heat-conducting manner to a cylinder, a cylinder head or a single pipe of the exhaust yas system.
The leeward side can be varied by changing the embodiment of the deflection surface in various ways. This may be linked to the wall and in this way form the smooth aerodynamic deflection device. According to other variations the wall is not part of the deflection device, but moreover is preferably constructed as a ridye roof, pointed hat, semi- to three quarter sphere or the like.
Briefly summarised once more, the essential advantages of the invention are found to be that - an oxygen probe, protected by a smooth, aerodynamic deflection device, with a high degree of heat resistance and a response time in the millisecond range allows a selective control of the cylinders, - measurements can take place without a reference atmosphere, and - the efficiency of the method is improved.
The smooth, aerodynamic deflection device, with or without oxygen probe, can be preassembled or fitted later.
The invention is explained in more detail with the aid of embodiment examples shown in the drawing, which are also the ~ubject of the dependent claims. Schematically shown are:
- Fig. 1 a perspective view of an exhaust system, ,:
: - . . ~ :
2 ~ 3 ~
- Fig. 2 a perspective view of an oxygen probe, - Fig. 3 a cut open single pipe with a protected probe, - Fig. 4 a cut open side view of Fig. 3, - Fig. 5 a cut open plan view of Fig. 3, and - Fig. 6 - 9 variations of smooth, aerodynamic deflection devices with an oxygen probe.
An exhaust system 10 shown in Fig. 1 comprises four single pipes 12 which are fixed to an engine flange 14. The single pipes 12 are combined into an exhaust manifold 16, a collecting pipe.
The exhaust manifold 16 feeds into a three-way catalyser 18 which reacts with about 90% efficiency with parts of carbon monoxide, nitrogen oxides and hydrocarbons, produced as a result of non-stoichiometric combustion in ~he hot exhaust gas stream 20, shown by an arrow, to form harmless gases.
A lambda probe 22 of conventional construction would be arranged in the area before the three-way catalyser 18 where th~ temperature of the exhaust gas stream has dropped to at least approximately 800C, as a rule to about 600C.
However, the exhaust system according to Fi.g. 1 does not contain the usual lambda probe 22 but, as shown in cletail in the Figs. 3 to 9, four resistive ceramic oxygen probes 24 protectecl by a smooth, aerodynamic deflection device with a high degree of heat resistance and adjustment time for each specific cylinder of approximately 5 msec.
Lambda probes 22 of conventional construction in the area of the single pipes 12, especially adjacent the engine flange 14, would no longer be functional and would be -destroyed because of excessively high temperatures if, for geometric reasons, they could be installed at all.
From each of the four oxygen probes 24 an electric conductor 26 leads to the electronics or the electronic control 28, where the measuring signals are converted into control signals for the mixture preparation and ignition (not shown)~
An oxygen probe 24 is shown in detail in Fig. ~. On a ceramic support 30 of dimensions from 5 x 4 x 0,8 mm is applied a thin diffusion layer of strontium titanate, the oxygen sensor 32. This diffusion layer, in the present case manufactured with the aid of thick-film technology, especially a screen printing technique, has a surface of approximately 6 to 8 mm2 and a thickness of approximately 8 to 10 ~m - shown in exaggerated strength. A fine-grained titanats ceramic powder applied to the aluminium oxide substrate, is burnt-on. The electric contact with the diffusion layer 32 is achieved through a thin coating of precious metal, which is also applie~ by screen printing as before.
For the manufacture of an even thinner diffusion layer 32, is also possible to use the thin-film technology known per se.
The operating current of the oxygen probe 24 is conducted via electric contacts through the diffusion layer which changes its electrical resistance in response to the oxygen partial pressure. The operating current is pre~erably d.c.
In the case of an automobi.le engine the usual car battery can be used as the current source without any converter units.
Beneath the ceramic support 30 are situated a meandering heating layer 36 and temperature sensor 38, shown only in .,.
." ~ ~ ~
20 5~ ~3 ~
part. Wlth a heating output of up to 5W, preferably also supplied by the car battery, the diffusion layer 32 can be heated to a temperature of approximately 600C through electrical resistance heating. As already mentioned, however, in the present invention this is of less significance because the oxygen probe has a low response temperature and is arranged in an area of high temperature.
Fig. 3 shows an enlarged cut-out from Fig. 1, but with a cut open single pipe 12. In the proximity of the engine flange 14, where the exhaust gas stream 20 enters the single pipe 12, is arranged a roof-shaped guide plate 40 which protects the oxygen probe 24 from the direct effect of the exhaust gas stream 20 and creates a region sheltered from the gas stream. This allows a homogenous but constantly renewing flow around the oxygen probe 24. The screening effect can be improved still further by the arrangement of a lateral screen 44 extending up to the ridge 42 running perpendicular to the pipe.
The Figs. 4 and 5 show even better the protection provided to the oxygen probe 24 by the roof-shaped deflection plate 40. The edges 46 of the deflection plate 40 situated downstream are bent outwards. This does not substantially impede the exhaust gas stream 20, but assists the homogenous flow around the oxygen probe.
In a single pipe 12 according to Fig. 6 is arranged a roof-shaped deflection plate 40 for an oxygen probe 24, which is shaped to run outwards in a concave manner.
In the region of the lower edges 46 of the deflection plate 40 the single pipe 12 has a bulge 48. This can prevent an exhaust gas build-up, which would reduce engine performance, because of the narrowing of the intermediate space as a result of the deflection plate 40 discharging relatively far on both sides. In the deflection plate 40 , : ' -~5~
according to Fig. 7, also constructed roof-shaped, for creating a region sheltered from the gas stream for an oxygen probe 24, the lower edges 46 are curled inwards.
The deflection plate 40 according to Fig. 8 i5 substantially spherical, with an opening situated downstream.
Finallyl in Fig. 9 the deflection plate 40 is constructed as a pointed hat. A counter piece 50 to the de1ection plate 40 is arranged downstream, also in the shape of a pointed hat. The already slight interference to the flow conditions can thus still be reduced by the arrangement of a deflection plate. Such counter pieces can of course also be used with roof-shaped or differently shaped deflection plates.
.
,
Control of the air ratio in a hot exhaust gas stream and oxygen probe therefore __________ _____________________________________________ The invention relates to a method for controlling the air-fuel mixture in an Otto engine having at least one cylinder, especially in an automobile engine, for the optimum use of a catalyser with a probe which serves to determine the air ratio in a hot exhaust gas stream with carbon monoxide, nitrogen oxides and hydrocarbons, in which the measuring signals of the probe are converted with an electronic means into control signals for the ignition and mixture preparation. The invention further relates to a d~vice for carrying out the method~
An Otto engine, an engine with a spark ignition, e.g. an automobile petrol engine, a stationary petrol engine or a two-stroke petrol engine, produces essentially carbon dioxide, but also carbon monoxide, nitrogen oxide and hydrocarbons, which are discharged into the environment.
Whereas the carbon monoxide and the nitrogen oxides relate to chemically defined compounds, the hydrocarbons comprise ; a large number of compo~nds.
Automobile engines especially these days are subjected to increasingly strict exhaust gas standards which permit only limited residual quantities of the harmful gases mentioned.
In khe exhaust gas cleaning technology for Otto engines driven by petrol, a central role is played by catalysers controlled by a lambda probe, especially three-way catalysers, but also oxidation andtor twin-bed catalysers.
In a series of chemical reactions, ~or example in a three-way catalyser, the harm~ul exhaust gas components, especially also the heterogenic hydrocarbons, are converted ;~ , , . , ~ . :
' ~, . p '.' . ' ' ' " . ~ 1'.". . , , :
2~8~2 are converted with approxima-tely 90% of efficiency into water, carbon dioxide, nitrogen and hydrogen.
The simultaneous reaction of the harmful exhaust gases of carbon monoxide, nitrogen oxides and hydrocarbons assumes that a ratio of the air-fuel mixture around the stoichiometric value ~ = 1 is adhered to within strict limits. Lambda is also used to represent the air ratio:
air quantity supplied = theoretical air requirement ~ < 1 refers to a rich mixture, ~ ~ 1 refers to a lean mixture.
A lambda probe supplies a voltage signal to an electronic control which in turn signals to a mixture preparation device whether the mixture is to be enriched or made leaner. However, the change in the air-fuel mixture must not take place suddenly, an integrator changes the mixture composition and, if necessary, it changes the ignition timing slowly as a function of time. The air-fuel mixture thus deviates constantly by a few percent around ~ = 1, even during optimum operation.
According to the present-day state of the art, lambda probes are arranged before the catalyser in the exhaust gas flow direction approximately lm down-stream behind the exhaust gas quarter bend, in the collecting pipe in the case of multi-cylinder engines~
A lambda probe operates according to the principle of a galvanic oxygen concentration cell with a solid body electrolyte of zirconium dioxide which is stabilised with yttrium oxide. The solid body electrolyte is protected with a metal mesh - also known as metal cage -, which dampens the force of the hot exhaust gas stream. The exhaust gas 2 ~
flows round the outer surface of the solid body electrolyte, while the inner open chamber is connected to the atmosphere as reference gas.
Despite its obvious advantages , the lambda probe also has disadvantages:
~ It operates only at temperatures from approximately 400C upwards. During the critical period prior to th0 catalyser being heated, the air-fuel mixture is not regulated, or the lambda probe must be pre-heated.
- The maximum continuous operating temperature is approximately 80~C. The probe must be arranged in a cooler area of the collecting pipe, relatively far back in the flow direction.
- The lamda probe has a response time of 50 to 100 msec.
which, together with the long delay of the exhaust gas prior to reaching the probe, amounts to a very long reaction time for engines operating at high speeds.
- The lambda probe provide~ with a metal mesh or metal cage has a large effective cross-section and therefore substantially inter~eres with the exhaust gas stream.
The CH-A5 666 724 describes a lambda probe which has a solid body electrolyte withdrawn from the exhaust gas stream. Whilst the lambda probe seated on a tubular holder is less likely to be overheated and does not interfere with the exhaust gas stream, being situated further back, however, it is even more sluggish with regard to the reaction time, the exhaust gas stream flowing unhindered no longer flows directly round the solid body electrolyte, but only after a branched-off partial stream has passed through a relatively small opening.
'~
;
5C~
The DE-Cl 3 743 295 sets out to prevent the probe ceramics from being destroyed by liquid droplets falling onto a heated lambda probe during cold starting. ~lso, the representation of the si~nals delivered by the lambda probe is intended to be improved. For this purpose a gas deflection plate is arranged upstream of the lambda probe in such a way that the lambda probe is situated in the flow shadow. The lambda probe protected by a relatively large cage of known construction is arranged in the collecting pipe of the exhaust system and captures part of the entire exhaust gas stream of all the cylinders in a region with an already relatively low gas temperature.
It is the object of the present invention to provide a method of the type mentioned at the beginning and a device for carrying the method which permit a more selective engine control with probes and associated control electronics which respond substantially more quickly than was hitherto the case.
With reference to the method, the object according to the invention is achieved in that the oxygen content of the exhaust gas stream is measured in the combustion chamber of the cylinders, after the outlet valve in the cylinder heads, or in the single pipes, by measuring without a re~erence atmosphere in the protective area of a smooth, aerodynamic deflection device with a resistive ceramic oxygen probe having a heat resistance of up to approximately 1300C and an adjustment time within the millisecond ~ange. Special and further developing embodiments are the subject of the dependent patent claims.
The deflection device arranged in the selective cylinder exhaust gas stream simultaneously carries out several functions:
, ~ , .
-- It forms a heat shield for the oxygen probe, which protects against the direct effect of the discharging exhaust gases of very high temperature produced in an explosion-like manner. However, the deflection device which is at least partly open in relation to the exhaust gases downstream in the flow direction ensures that directly and unmixed a part of the exhaust gas stream always flows around the probe. With the oxygen probe arranged in a completely closed or substantially closed deflection device, the advantage of a quick response time would be at least partly cancelled out, similar to an arrangement of a probe according to CH-AS 666724.
- The metal deflection device removes heat from the protective region for the oxygen probe situated in the exhaust gas stream and conducts this to the outside. This improves the heat protection still further.
- Because of the mall dimensions of the probe, the exhaust gas stream is only insignificantly affected even in single pipes by the small construction of the smooth, aerodynamic deflection device and therefore does not af~ect engine efficiency or only insignificantly.
A conventional lambda probe with the necessary protective cage for purely geometric reasons alone could not be arranged in an single pipe and despite deflection plate would never be able to withstand the high temperatures of the method according to the invention.
According to the invention, the oxygen content is measured with an adjustment time of 1 to 20 msec, preferably 3 to 15 msec. With a response time of a few milliseconds, the resistive oxygen probe can measure and adjust the air-fuel mixture of each individual piston stroke even in engines running at high speeds, for example 6000 revolutions per minute. For dynamic drive situations, especially when :~
- . , : ~.
- :~
2 ~
accelerating, with a downstream catalyser the fuel consumption and thus the emission of harmful exhaust gases can be reduced to a minimum. In the first place this is of great significance during the cold starting phase, during which a short response time is essential.
The high degree of heat resistance of the oxygen sensor operating without a reference atmosphere, in cooperation with the smooth, aerodynamic deflection device, allo~s the oxygen content to be measured in the combustion chamber of the cylinders, after the outlet valve in the cylinder heads or in the single pipes of the exhaust system. Of particular practical interest is the measurement of the oxygen ratio directly after the inlet opening of an single pipe of the exhaust system. Only these measuring points, situated outside the operating area of the conventional lambda probes, allow a selected cylinder to be controlled, i.e.
the optîmum combustion in each cylinder.
For the sake of completeness, it is emphasised once more that with the classical lambda probes the oxygen content of the exhaust gas stream can only be measured in the collecting pipe of the exhaust system Because of the deflection device, the oxygen probe as a rule has an adequate heat resistance up to approximately 1300C even in very hot parts of the engine. In the said preferred re~ion for measuring the oxygen content, the inlet region to the single pipes, the temperature as a rule is around 900 to 1100C.
Although resistive ceramic oxygen probes start to react at a temperature of 20C, an arrangement in hot to very hot exhaust gases i6 advantageous, because the delay time is shortest after ignition of the gases until the exhaust i gases reach the oxygen probe and, for adjusting the oxygen : . ~ ,, ~
,, , :. - , , :
2~5~
content, the optimum permanent temperature of the oxygen probe for regulating the air-fuel mixture is quickly reached.
The further simplification of the measuring method is helped by the fact that a resistive oxygen probe operating without a reference atmosphere, apart from high temperatures, is also resistant to high pressures without affecting the quick response time within the millisecond range.
With reference to the device, the object is achieved according to the invention in that an oxygen probe with specific electrical conductivity dependent on the oxygen partial pressure, as the thin diffusion layer of a semi-conducting titanate on a small ceramic support, is arranged on the leeward side of an aerodynamic deflection surface which is at least partly open downstream in the combustion chamber of the cylinder, after the outlet valve in the cylinder heads or in the single pipes. Special and further developing embodiments are the subject of the dependent patent claims.
The active layer of the oxygen sensor preferably has a two-dimensional expansion of from 0,5 to 10 mm2 and a thickness of 1 to 20 ~m, especially 5 to 10 ~m. The application preferably takes place by thin or thick-film technology.
An oxygen sensor of small dimensions, which is known per se and which is freely available, is of considerable significance for a number of reasons:
:' .
- The sensor adjustment time i6 dependent on the layer thickness; the thinner the layer, the shorter the adjustment time.
i ~ - The flow behaviour of the exhaust gases should be .. ~
.--- ..
.
2 ~
disturbed as little as possible by the oxygen probe. This can best be achieved by a deflection surface in which the sensor to be protected is as small as possible. The closer the oxygen probe is arranged to a combustion chamber, the more important become flow optimisation and thus, according to the invention, an 0ffective combination of deflection surface and oxygen probe for producing a homogenous flow around the same.
- Smaller oxygen probes and thus smaller deflection surfaces result in smaller manufacturing and assembly costs.
The diffusion layer which absorbs oxygen in proportion to the partial pressure preferably consists of calcium, strontium or barium titanate with doping material known per se. The conductivity as a function of the oxygen partial pressure is the result of a change in the concentration of atomic defects. Because of its direct dependence on the oxygen partial pressure, this electric conductivity requires no reference atmosphere.
Newly fitted or exchanged oxygen probes preferably have an oxygen-absorbing diffusion layer which already contains the impurities present in the exhaust gas stream. A balance therefore always exists right from the start, which therefore immediately allows an optimum adjustment of the oxygen content even during a refit.
The oxygen probe and the deflection surface are preferably constructed as one module to be rigidly fitted or which can preferably be exchanged.
The deflection surface is made from a heat-resistant and corrosion-proof material which is also abrasion-resistant, preferably from a metal and/or ceramic material which is smooth and aerodynamically shaped in order to reduce the 2 ~ r~ 2 flow resistance. A deflection plate, e.g. forming the deflection surface, made from metal, preferably a heat-conducting steel or a copper alloy is preferably connected in a heat-conducting manner to a cylinder, a cylinder head or a single pipe of the exhaust yas system.
The leeward side can be varied by changing the embodiment of the deflection surface in various ways. This may be linked to the wall and in this way form the smooth aerodynamic deflection device. According to other variations the wall is not part of the deflection device, but moreover is preferably constructed as a ridye roof, pointed hat, semi- to three quarter sphere or the like.
Briefly summarised once more, the essential advantages of the invention are found to be that - an oxygen probe, protected by a smooth, aerodynamic deflection device, with a high degree of heat resistance and a response time in the millisecond range allows a selective control of the cylinders, - measurements can take place without a reference atmosphere, and - the efficiency of the method is improved.
The smooth, aerodynamic deflection device, with or without oxygen probe, can be preassembled or fitted later.
The invention is explained in more detail with the aid of embodiment examples shown in the drawing, which are also the ~ubject of the dependent claims. Schematically shown are:
- Fig. 1 a perspective view of an exhaust system, ,:
: - . . ~ :
2 ~ 3 ~
- Fig. 2 a perspective view of an oxygen probe, - Fig. 3 a cut open single pipe with a protected probe, - Fig. 4 a cut open side view of Fig. 3, - Fig. 5 a cut open plan view of Fig. 3, and - Fig. 6 - 9 variations of smooth, aerodynamic deflection devices with an oxygen probe.
An exhaust system 10 shown in Fig. 1 comprises four single pipes 12 which are fixed to an engine flange 14. The single pipes 12 are combined into an exhaust manifold 16, a collecting pipe.
The exhaust manifold 16 feeds into a three-way catalyser 18 which reacts with about 90% efficiency with parts of carbon monoxide, nitrogen oxides and hydrocarbons, produced as a result of non-stoichiometric combustion in ~he hot exhaust gas stream 20, shown by an arrow, to form harmless gases.
A lambda probe 22 of conventional construction would be arranged in the area before the three-way catalyser 18 where th~ temperature of the exhaust gas stream has dropped to at least approximately 800C, as a rule to about 600C.
However, the exhaust system according to Fi.g. 1 does not contain the usual lambda probe 22 but, as shown in cletail in the Figs. 3 to 9, four resistive ceramic oxygen probes 24 protectecl by a smooth, aerodynamic deflection device with a high degree of heat resistance and adjustment time for each specific cylinder of approximately 5 msec.
Lambda probes 22 of conventional construction in the area of the single pipes 12, especially adjacent the engine flange 14, would no longer be functional and would be -destroyed because of excessively high temperatures if, for geometric reasons, they could be installed at all.
From each of the four oxygen probes 24 an electric conductor 26 leads to the electronics or the electronic control 28, where the measuring signals are converted into control signals for the mixture preparation and ignition (not shown)~
An oxygen probe 24 is shown in detail in Fig. ~. On a ceramic support 30 of dimensions from 5 x 4 x 0,8 mm is applied a thin diffusion layer of strontium titanate, the oxygen sensor 32. This diffusion layer, in the present case manufactured with the aid of thick-film technology, especially a screen printing technique, has a surface of approximately 6 to 8 mm2 and a thickness of approximately 8 to 10 ~m - shown in exaggerated strength. A fine-grained titanats ceramic powder applied to the aluminium oxide substrate, is burnt-on. The electric contact with the diffusion layer 32 is achieved through a thin coating of precious metal, which is also applie~ by screen printing as before.
For the manufacture of an even thinner diffusion layer 32, is also possible to use the thin-film technology known per se.
The operating current of the oxygen probe 24 is conducted via electric contacts through the diffusion layer which changes its electrical resistance in response to the oxygen partial pressure. The operating current is pre~erably d.c.
In the case of an automobi.le engine the usual car battery can be used as the current source without any converter units.
Beneath the ceramic support 30 are situated a meandering heating layer 36 and temperature sensor 38, shown only in .,.
." ~ ~ ~
20 5~ ~3 ~
part. Wlth a heating output of up to 5W, preferably also supplied by the car battery, the diffusion layer 32 can be heated to a temperature of approximately 600C through electrical resistance heating. As already mentioned, however, in the present invention this is of less significance because the oxygen probe has a low response temperature and is arranged in an area of high temperature.
Fig. 3 shows an enlarged cut-out from Fig. 1, but with a cut open single pipe 12. In the proximity of the engine flange 14, where the exhaust gas stream 20 enters the single pipe 12, is arranged a roof-shaped guide plate 40 which protects the oxygen probe 24 from the direct effect of the exhaust gas stream 20 and creates a region sheltered from the gas stream. This allows a homogenous but constantly renewing flow around the oxygen probe 24. The screening effect can be improved still further by the arrangement of a lateral screen 44 extending up to the ridge 42 running perpendicular to the pipe.
The Figs. 4 and 5 show even better the protection provided to the oxygen probe 24 by the roof-shaped deflection plate 40. The edges 46 of the deflection plate 40 situated downstream are bent outwards. This does not substantially impede the exhaust gas stream 20, but assists the homogenous flow around the oxygen probe.
In a single pipe 12 according to Fig. 6 is arranged a roof-shaped deflection plate 40 for an oxygen probe 24, which is shaped to run outwards in a concave manner.
In the region of the lower edges 46 of the deflection plate 40 the single pipe 12 has a bulge 48. This can prevent an exhaust gas build-up, which would reduce engine performance, because of the narrowing of the intermediate space as a result of the deflection plate 40 discharging relatively far on both sides. In the deflection plate 40 , : ' -~5~
according to Fig. 7, also constructed roof-shaped, for creating a region sheltered from the gas stream for an oxygen probe 24, the lower edges 46 are curled inwards.
The deflection plate 40 according to Fig. 8 i5 substantially spherical, with an opening situated downstream.
Finallyl in Fig. 9 the deflection plate 40 is constructed as a pointed hat. A counter piece 50 to the de1ection plate 40 is arranged downstream, also in the shape of a pointed hat. The already slight interference to the flow conditions can thus still be reduced by the arrangement of a deflection plate. Such counter pieces can of course also be used with roof-shaped or differently shaped deflection plates.
.
,
Claims (10)
1. Method for controlling the air-fuel mixture in an Otto engine having at least one cylinder, especially in an automobile engine, for the optimum use of a catalyser (18) with a probe which serves to determine the air ratio ( ) in a hot exhaust gas stream (20) with carbon monoxide, nitrogen oxides and hydrocarbons, in which the measuring signals of the probe are converted with an electronic means (28) into control signals for the ignition and mixture preparation, characterised in that the oxygen content of the exhaust gas stream (20) is measured in the combustion chamber of the cylinders, after the outlet valve in the cylinder heads, or in the single pipes, by measuring without a reference atmosphere in the protective area of a smooth, aerodynamic deflection device (40) with a resistive ceramic oxygen probe (24) having a heat resistance of up to approximately 1300°C and an adjustment time within the millisecond range.
2. Method according to claim 1, characterised in that the oxygen content is measured with an oxygen probe (24) having a adjustment time of 1 to 20 msec, preferably 3 to 15 msec, at a temperature of 1200°C, preferably 900 to 1100°C.
3. Method according to claim 1 or 2, characterised in that the oxygen content is measured directly after the inlet opening to the single pipes (12).
4. Device for carrying out the method according to one of the claims 1 to 3, characterised in that an oxygen probe (24) with specific electrical conductivity dependent on the oxygen partial pressure, as the thin diffusion layer (32) of a semi-conducting titanate on a small ceramic support (30), is arranged on the leeward side of an aerodynamic deflection surface (40) which is at least partly open downstream in the combustion chamber of the cylinder, after the outlet valve in the cylinder heads or in the single pipes (12).
5. Device according to claim 4, characterised in that the oxygen-absorbing diffusion layer, the sensor layer (32) consists of calcium, strontium or barium titanate, has a planar expansion of 0,5 to 10 mm2 and a thickness of preferably 1 to 20 µm, especially 5 to 10 µm.
6. Device according to claim 4 or 5, characterised in that the oxygen-absorbing diffusion layer (32) of a newly installed or exchanged oxygen probe (24) contains in equal concentration by weight the impurities present in the exhaust gas stream (20).
7. Device according to one of the claims 4 to 6, characterised in that the oxygen probe (24) is equipped with a heating meander (36) and/or a temperature sensor (38).
8. Device according to one of the claims 4 to 7, characterised in that the oxygen probe (24) and the deflection surface (40) are constructed as one built-in module.
9. Device according to one of the claims 4 to 8, characterised in that the deflection surface (40) consists of a heat resistant, corrosion-proof metal sheet and is connected in a heat conducting manner to a single pipe (12) opening.
10. Device according to one of the claims 4 to 9, characterised in that the deflection surface (40) is roof-shaped with a ridge (42) running approximately perpendicularly to the wall, also with concave running roof surfaces, or is constructed as a pointed hat or as a semi to three-quarter sphere, in which the edges (46) situated downstream are also bent inwards or outwards.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH1444/90A CH682340A5 (en) | 1990-04-27 | 1990-04-27 | |
CH1444/90-4 | 1990-04-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2058452A1 true CA2058452A1 (en) | 1991-10-28 |
Family
ID=4210608
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002058452A Abandoned CA2058452A1 (en) | 1990-04-27 | 1991-04-22 | Process for controlling the proportion of air in a hot exhaust-gas stream, and oxygen probe for use in the process |
Country Status (11)
Country | Link |
---|---|
US (1) | US5226921A (en) |
EP (1) | EP0483303B1 (en) |
JP (1) | JPH04506869A (en) |
KR (1) | KR920702774A (en) |
AT (1) | ATE132628T1 (en) |
AU (1) | AU7664091A (en) |
BR (1) | BR9105727A (en) |
CA (1) | CA2058452A1 (en) |
CH (1) | CH682340A5 (en) |
DE (1) | DE59107202D1 (en) |
WO (1) | WO1991017434A1 (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
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US5582156A (en) * | 1993-01-25 | 1996-12-10 | Brqt Corporation | Two-cycle internal combustion engine with reduced unburned hydrocarbons in the exhaust gas and adjustable spark gap electrodes |
US5311854A (en) * | 1993-01-25 | 1994-05-17 | Brqt Corporation | Two-cycle internal combustion engine with reduced unburned hydrocarbons in the exhaust gas |
US5388561A (en) * | 1993-01-25 | 1995-02-14 | Brqt Corporation | Two-cycle internal combustion engine with reduced unburned hydrocarbons in the exhaust gas and adjustable spark gap electrodes |
JP2007046463A (en) * | 2005-08-05 | 2007-02-22 | Yamaha Motor Co Ltd | Exhaust system, and engine and vehicle equipped with it |
JP6127395B2 (en) * | 2012-06-29 | 2017-05-17 | 三菱自動車工業株式会社 | Sensor protection structure |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4055792A (en) * | 1974-07-01 | 1977-10-25 | Ford Motor Company | Electrical control system for an exhaust gas sensor |
JPS5629738Y2 (en) * | 1976-09-21 | 1981-07-15 | ||
JPS5627831A (en) * | 1979-08-14 | 1981-03-18 | Matsushita Electric Ind Co Ltd | Combustion safety device |
US4377143A (en) * | 1980-11-20 | 1983-03-22 | Ford Motor Company | Lean air-fuel control using stoichiometric air-fuel sensors |
DE3203200A1 (en) * | 1982-01-30 | 1983-08-04 | Bosch Gmbh Robert | Spark plug with oxygen sensor |
JPS58148946A (en) * | 1982-02-27 | 1983-09-05 | Nissan Motor Co Ltd | air fuel ratio detector |
DE3238753A1 (en) * | 1982-10-20 | 1984-04-26 | Robert Bosch Gmbh, 7000 Stuttgart | METHOD AND DEVICE FOR REGULATING THE FUEL-AIR MIXTURE TO BE ADDED TO AN INTERNAL COMBUSTION ENGINE |
JPS604850A (en) * | 1983-06-23 | 1985-01-11 | Ngk Spark Plug Co Ltd | Oxygen sensor |
JPH0652057B2 (en) * | 1984-05-07 | 1994-07-06 | トヨタ自動車株式会社 | Internal combustion engine controller |
JPS61147146A (en) * | 1984-12-20 | 1986-07-04 | Fuigaro Giken Kk | Lambda sensor |
JPS6388244A (en) * | 1986-09-30 | 1988-04-19 | Mitsubishi Electric Corp | Air-fuel ratio control device |
US4957705A (en) * | 1986-11-10 | 1990-09-18 | Japan Electronic Control Systems Co., Ltd. | Oxygen gas concentration-detecting apparatus |
JP2797306B2 (en) * | 1987-03-13 | 1998-09-17 | 三菱自動車工業株式会社 | Oxygen sensor and air-fuel ratio control device for internal combustion engine using the sensor |
JPH01147138A (en) * | 1987-12-01 | 1989-06-08 | Mitsubishi Electric Corp | Heater controller for air-fuel ratio sensor |
DE3743295C1 (en) * | 1987-12-19 | 1988-07-07 | Daimler Benz Ag | Device for prolonging the service life and improving the measurement presence of a lambda probe installed in the exhaust gas flow of an internal combustion engine |
DE3805734A1 (en) * | 1988-02-24 | 1989-08-31 | Bosch Gmbh Robert | USE OF ZEOLITES AS SPECIFIC ADSORBENTS FOR NO (DOWN ARROW) X (DOWN ARROW) AND CO |
-
1990
- 1990-04-27 CH CH1444/90A patent/CH682340A5/de not_active IP Right Cessation
-
1991
- 1991-04-22 KR KR1019910701983A patent/KR920702774A/en not_active Withdrawn
- 1991-04-22 BR BR919105727A patent/BR9105727A/en not_active Application Discontinuation
- 1991-04-22 US US07/793,361 patent/US5226921A/en not_active Expired - Fee Related
- 1991-04-22 AU AU76640/91A patent/AU7664091A/en not_active Abandoned
- 1991-04-22 EP EP91907551A patent/EP0483303B1/en not_active Expired - Lifetime
- 1991-04-22 DE DE59107202T patent/DE59107202D1/en not_active Expired - Fee Related
- 1991-04-22 CA CA002058452A patent/CA2058452A1/en not_active Abandoned
- 1991-04-22 WO PCT/CH1991/000092 patent/WO1991017434A1/en active IP Right Grant
- 1991-04-22 JP JP3506717A patent/JPH04506869A/en active Pending
- 1991-04-22 AT AT91907551T patent/ATE132628T1/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
JPH04506869A (en) | 1992-11-26 |
CH682340A5 (en) | 1993-08-31 |
US5226921A (en) | 1993-07-13 |
EP0483303B1 (en) | 1996-01-03 |
ATE132628T1 (en) | 1996-01-15 |
DE59107202D1 (en) | 1996-02-15 |
EP0483303A1 (en) | 1992-05-06 |
BR9105727A (en) | 1992-05-19 |
KR920702774A (en) | 1992-10-06 |
WO1991017434A1 (en) | 1991-11-14 |
AU7664091A (en) | 1991-11-27 |
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Legal Events
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FZDE | Discontinued |